Evidence map›Paper›PMID 34505396›Full record

ArticleCancer medicine2021

Severe anaphylaxis caused by intravenous anti-cancer drugs.

Nobuyuki Horita, Etsuko Miyagi, Taichi Mizushima, Maki Hagihara, Chiaki Hata, Yuki Hattori, Narihiko Hayashi, Kuniyasu Irie, Hideyuki Ishikawa, Yusuke Kawabata and 17 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.8field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Successful desensitization to etoposide in a patient after cardiac arrest.Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners · 2025
    Article
  5. Article
  6. Immune Reactions in Major Types of Oncological Treatment.International journal of molecular sciences · 2023
    Review
  7. Article
  8. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

27 authors at 1 institution in 1 country.

Nobuyuki HoritaChemotherapy Committee, Yokohama City University Hospital, Yokohama, Japan.ORCID 0000-0002-8200-0340
Etsuko MiyagiDepartment of Obstetrics and Gynecology, Yokohama City University Hospital, Yokohama, Japan.
Taichi MizushimaChemotherapy Committee, Yokohama City University Hospital, Yokohama, Japan.
Maki HagiharaChemotherapy Committee, Yokohama City University Hospital, Yokohama, Japan.
Chiaki HataChemotherapy Committee, Yokohama City University Hospital, Yokohama, Japan.
Yuki HattoriChemotherapy Committee, Yokohama City University Hospital, Yokohama, Japan.
Narihiko HayashiChemotherapy Committee, Yokohama City University Hospital, Yokohama, Japan.
Kuniyasu IrieChemotherapy Committee, Yokohama City University Hospital, Yokohama, Japan.
Hideyuki IshikawaChemotherapy Committee, Yokohama City University Hospital, Yokohama, Japan.
Yusuke KawabataChemotherapy Committee, Yokohama City University Hospital, Yokohama, Japan.
Yosuke KitaniChemotherapy Committee, Yokohama City University Hospital, Yokohama, Japan.
Noritoshi KobayashiChemotherapy Committee, Yokohama City University Hospital, Yokohama, Japan.
Nobuaki KobayashiChemotherapy Committee, Yokohama City University Hospital, Yokohama, Japan.
Yusuke KuritaChemotherapy Committee, Yokohama City University Hospital, Yokohama, Japan.
Yohei MiyakeChemotherapy Committee, Yokohama City University Hospital, Yokohama, Japan.
Kentaro MiyakeChemotherapy Committee, Yokohama City University Hospital, Yokohama, Japan.
Senri OguriChemotherapy Committee, Yokohama City University Hospital, Yokohama, Japan.
Ichiro OtaChemotherapy Committee, Yokohama City University Hospital, Yokohama, Japan.
Ayako ShimizuChemotherapy Committee, Yokohama City University Hospital, Yokohama, Japan.
Masanobu TakeuchiChemotherapy Committee, Yokohama City University Hospital, Yokohama, Japan.
Akimitsu YamadaChemotherapy Committee, Yokohama City University Hospital, Yokohama, Japan.
Kojiro YamamotoChemotherapy Committee, Yokohama City University Hospital, Yokohama, Japan.
Norio YukawaChemotherapy Committee, Yokohama City University Hospital, Yokohama, Japan.
Munetaka MasudaDepartment of Surgery, Yokohama City University Hospital, Yokohama, Japan.
Nobuhiko OridateDepartment of Otorhinolaryngology Head and Neck Surgery, Yokohama City University Hospital, Yokohama, Japan.
Yasushi IchikawaDepartment of Oncology, Yokohama City University Hospital, Yokohama, Japan.
Takeshi KanekoDepartment of Pulmonology, Yokohama City University Hospital, Yokohama, Japan.
Yokohama City University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe incidence and risk factors of severe anaphylaxis by intravenous anti-cancer drugs are unclear, whereas those of milder reactions have been reported. STUDY

designElectronic medical charts of cancer patients who have undergone intravenous chemotherapy between January 2013 and October 2020 in a university hospital were retrospectively reviewed. Non-epithelial malignancies were also included in the analysis. "Severe anaphylaxis" was judged using Brown's criteria: typical presentation of anaphylaxis and one or more of hypoxia, shock, and neurologic compromise. (UMIN000042887).

resultsAmong 5584 patients (2964 males [53.1%], 2620 females [46.9%], median age 66 years), 88,200 person-day anti-cancer drug administrations were performed intravenously, and 27 severe anaphylaxes were observed. The causative drugs included carboplatin (14 cases), paclitaxel (9 cases), and cisplatin, docetaxel, trastuzumab, and cetuximab (1 case each). The person-based lifetime incidence of severe anaphylaxis for patients who received at least one intravenous chemotherapy was 0.48% (27/5584, 95% confidence interval (CI) 0.30%-0.67%) and the administration-based incidence was 0.031% (27/88,200, 95% CI 0.019%-0.043%). Among 124 patients who received at least 10 carboplatin administrations, 10 patients experienced carboplatin-induced severe anaphylaxis (10/124, 8.1%, 95% CI 3.0%-13.1%). Carboplatin caused severe anaphylaxis after at least 9-min interval since the drip started. Thirteen out of 14 patients experienced carboplatin-induced severe anaphylaxis within a 75-day interval from the previous treatment. Paclitaxel infusion caused severe anaphylaxis after a median of 5 min after the first drip of the day at a life-long incidence of 0.93% (9/968, 95% CI 0.27%-1.59%).

conclusionWe elucidated the high-risk settings of chemotherapy-induced severe anaphylaxis.

Indexed as

Administration, IntravenousAgedAnaphylaxisAntineoplastic AgentsFemaleHumansIncidenceMaleMiddle AgedRetrospective StudiesRisk FactorsAntineoplastic Agentsanaphylaxisdrug hypersensitivitymedical oncologyretrospective studies

Identifiers

PMID34505396
PMCPMC8525120
OpenAlexW3197581154

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.